Badis Yacine, Bonhomme Maxime, Lafitte Claude, Huguet Stéphanie, Balzergue Sandrine, Dumas Bernard, Jacquet Christophe
Laboratoire de Recherche en Sciences Végétales, UPS, Université de Toulouse, BP42617, Auzeville, F-31326, Castanet-Tolosan, France.
Laboratoire de Recherche en Sciences Végétales, CNRS, BP42617, Auzeville, F-31326, Castanet-Tolosan, France.
Mol Plant Pathol. 2015 Dec;16(9):973-86. doi: 10.1111/mpp.12253. Epub 2015 May 4.
To gain an insight into the molecular mechanisms of quantitative disease resistance in Medicago truncatula to the root-infecting oomycete Aphanomyces euteiches, we selected two near-isogenic lines (NILs), NR and NS, partially resistant and susceptible, respectively, differing in the allelic state of the quantitative resistance locus (QRL) prAe1 (partially resistant to A. euteiches 1). Complementary molecular and cytological phenotyping methods showed that prAe1 alone confers quantitative resistance to A. euteiches. Root and stem tissues were colonized in NS plants and 80% of NS plants died by 21 days post-inoculation (dpi). In contrast, A. euteiches mycelium was restricted to the root cortex and the spread of symptoms was arrested in aerial parts of NR plants. A transcriptome analysis performed at 0, 1 and 6 dpi identified 1198 differentially expressed genes (DEGs) between NR and NS lines. More than 87% of the DEGs were significantly more expressed in NR. The highest number of DEGs was found in control conditions, with 723 genes over-expressed in NR versus 85 in NS. Genes belonging to secondary metabolism, pathogenesis-related (PR) proteins and kinases were significantly enriched. The significant role of the flavonoid pathway in resistance was corroborated by the detection of larger amounts of flavonoids in NR roots and the inhibition of A. euteiches zoospore germination by 2'-O-methyl-isoliquiritigenin, a compound synthesized by enzymes specifically induced in NR. Our study revealed that prAe1-dependent resistance relies mainly on the constitutive expression of defence-related pathways and signalling elements, which can be re-amplified in later time points of the infection.
为深入了解蒺藜苜蓿对根部感染卵菌大豆疫霉的数量抗病性的分子机制,我们选择了两个近等基因系(NILs),即NR和NS,分别为部分抗性和易感,它们在数量抗性位点(QRL)prAe1(对大豆疫霉1部分抗性)的等位基因状态上存在差异。互补的分子和细胞表型分析方法表明,单独的prAe1赋予对大豆疫霉的数量抗性。NS植株的根和茎组织被定殖,80%的NS植株在接种后21天(dpi)死亡。相比之下,大豆疫霉的菌丝体局限于根皮层,症状在NR植株地上部分的蔓延被阻止。在0、1和6 dpi进行的转录组分析确定了NR和NS系之间1198个差异表达基因(DEGs)。超过87%的DEGs在NR中表达显著更高。在对照条件下发现的DEGs数量最多,NR中有723个基因过度表达,而NS中为85个。属于次生代谢、病程相关(PR)蛋白和激酶的基因显著富集。NR根中检测到大量黄酮类化合物,以及2'-O-甲基异甘草素(一种由NR中特异性诱导的酶合成的化合物)对大豆疫霉游动孢子萌发的抑制作用,证实了黄酮类途径在抗性中的重要作用。我们的研究表明,prAe1依赖性抗性主要依赖于防御相关途径和信号元件的组成型表达,这些在感染的后期时间点可以再次放大。